Organic Chemistry Reaction Mechanisms: Electrophilic Addition and Free Radicals

Understanding how molecules interact and transform is the key to mastering organic chemistry. This text-based course breaks down complex organic reaction pathways into clear, logical steps, helping you build a strong foundation in chemical reactivity. You will start with the essential terminology, electronic effects, and stability principles before diving deep into specific reaction pathways. Through clear explanations and step-by-step written walkthroughs, you will learn to predict reaction outcomes, write out intermediate steps, and understand the driving forces behind chemical transformations. This course focuses heavily on Electrophilic Addition Reactions (EAR) and free radical pathways, which are essential for pre-medical examinations and foundational college chemistry. What you'll learn: - Understand the core principles of reaction intermediates, including carbocation stability and radical formation - Analyze Electrophilic Addition Reactions (EAR) in alkenes and alkynes step-by-step - Master free radical mechanisms, including halogenation, initiation, propagation, and termination steps - Predict major and minor products of organic reactions using Markovnikov and anti-Markovnikov rules - Apply modern structural concepts and stereochemical outcomes to reaction pathways The course begins with foundational definitions of nucleophiles, electrophiles, and intermediates, then guides you through detailed mechanical pathways, and concludes with practical problem-solving strategies to help you tackle exam-style questions with confidence. This course is designed for beginner to intermediate chemistry students and pre-medical aspirants who want to build a deep, conceptual understanding of organic mechanisms without relying on rote memorization. No advanced organic chemistry knowledge is required to start.